NDC codes

FDA NDC Directory
Product NDC (as listed)73107-105Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73107-0105Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
73107-105-30731070105307310701053030 mL in 1 BOTTLE (73107-105-30)Marketed from May 12, 2020
73107-105-31731070105317310701053150 mL in 1 BOTTLE (73107-105-31)Marketed from May 12, 2020
73107-105-32731070105327310701053285 mL in 1 BOTTLE (73107-105-32)Marketed from May 12, 2020
73107-105-337310701053373107010533100 mL in 1 BOTTLE (73107-105-33)Marketed from May 12, 2020
73107-105-347310701053473107010534150 mL in 1 BOTTLE (73107-105-34)Marketed from May 12, 2020
73107-105-357310701053573107010535200 mL in 1 BOTTLE (73107-105-35)Marketed from May 12, 2020
73107-105-367310701053673107010536250 mL in 1 BOTTLE (73107-105-36)Marketed from May 12, 2020
73107-105-377310701053773107010537500 mL in 1 BOTTLE (73107-105-37)Marketed from May 12, 2020
73107-105-3873107010538731070105381000 mL in 1 BOTTLE (73107-105-38)Marketed from May 12, 2020
73107-105-3973107010539731070105395000 mL in 1 BOTTLE (73107-105-39)Marketed from May 12, 2020
73107-105-4073107010540731070105405 mL in 1 PACKET (73107-105-40)Marketed from May 12, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
KONIX Alcohol Antiseptic Hand Rub
Generic name (nonproprietary)
konix alcohol antiseptic hand rub
Active ingredients
Alcohol — 70 mL/100mL
Dosage form
Solution
Route
Topical
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication part333A
Marketing start
Listing expires
Identifiers
Product ID 73107-105_d8939fbd-da34-4f20-ab23-2d4b7fd62363SPL ID d8939fbd-da34-4f20-ab23-2d4b7fd62363SPL set ID 17435b35-815b-4292-a809-e533ea137b80RxCUI 582753UNII 3K9958V90MUPC 8681715344874, 8681715344799, 8681715344775, 8681715344843, 8681715344829, 8681715344812, 8681715344867, 8681715344805, 8681715344850, 8681715344782, 8681715344836

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473107010530 followed by a unit qualifier and the quantity

Package 73107-0105-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Use Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73107-105

What is NDC 73107-105?
73107-105 is the product NDC for KONIX Alcohol Antiseptic Hand Rub, Alcohol 70 mL/100mL solution, listed with the FDA by TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS. It has 11 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
KONIX Alcohol Antiseptic Hand Rub.
What is the active ingredient?
Alcohol.
Who is the labeler?
TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS, NDC labeler code 73107. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for KONIX Alcohol Antiseptic Hand Rub?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under part333A

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under part333A
ProductStrengthForm · routeLabelerProduct NDC
Foaming Mousse Anti-Bacterial Hand Sanitizer Cherry ScentedalcoholAlcohol 62 mL/100mLAerosol, FoamTopicalGanzhou Olivee Cosmetic Co., Ltd.56136-021
Antimicrobial Hand WashchloroxylenolChloroxylenol 6 mg/1000mLSoapTopicalHenry Schein, Inc.0404-5990
TOUCH Sanitizing Germ Block, Ocean Mist, 1oz (28.35g)benzalkonium chlorideBenzalkonium chloride .13 g/100gAerosol, SprayTopicalRelevo, Inc.69744-0204
Hand Wipeschlorhexidine digluconate and benzethonium chlorideChlorhexidine gluconate .1 g/g; Benzethonium chloride .08 g/gClothTopicalJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.71734-203
Callington Anti-Bacterial Hand Sanitiserbenzalkonium chlorideBenzalkonium chloride .05 g/gClothTopicalJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.71734-210
CPAP Mask cleaning wipesbenzethonium chloride and benzalkonium chlorideBenzethonium chloride .03 g/g; Benzalkonium chloride .02 g/gClothTopicalJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.71734-212
Antimicrobial Hand WashchloroxylenolChloroxylenol 6 mg/1000mLSoapTopicalHenry Schein, Inc.0404-5987
HydrAphexBenzalkonium chloride .0013 g/mLSolutionTopicalAphex Biocleanse Systems, Inc78003-140
Byotrol Hand Sanitizerbenzalkonium chlorideBenzalkonium chloride 1.3 mg/mLLiquidTopicalAdvanced Hygienics LLC63002-002
Hand Sanitizerbenzalkonium chlorideBenzalkonium chloride 1.3 g/mLSolutionTopicalAdvanced Hygienics LLC63002-004
Foaming Mousse Anti-Bacterial Hand Sanitizer Pineapple ScentedalcoholAlcohol 62 mL/100mLAerosol, FoamTopicalGanzhou Olivee Cosmetic Co., Ltd.56136-022
Foaming Mousse Anti-Bacterial Hand Sanitizer Pink Grapefruit ScentedalcoholAlcohol 62 mL/100mLAerosol, FoamTopicalGanzhou Olivee Cosmetic Co., Ltd.56136-023
CVS Hand SanitizeralcoholAlcohol 56 mg/gSprayTopicalCVS69842-557
BZK Towelettebenzalkonium chlorideBenzalkonium chloride 1.33 mg/mLSwabTopicalAcme United Corporation0924-7112
MistalcoholAlcohol 62 mL/100mLSprayTopicalDerma Glove70741-003
MistalcoholAlcohol 62 mL/100mLSprayTopicalDerma Glove70741-003
MistalcoholAlcohol 62 mL/100mLSprayTopicalDerma Glove70741-003
MistalcoholAlcohol 62 mL/100mLSprayTopicalDerma Glove70741-003
HandlotionAlcohol 70 mL/100mLLotionTopicalDerma Glove70741-006
Soft Care Sentrybenzalkonium chlorideBenzalkonium chloride .13 g/100mLSolutionTopicalDiversey, Inc.64536-1948

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